Canonical Allele Identifier: PA177080
Gene: MYH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 164431
ClinVar RCV Id: RCV000151325 RCV000727282 RCV002483309 RCV004532678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002464.1:p.Ser1519Asn
CA177078
NM_002473.6:c.4556G>A